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Clinical diagnosis and treatment of 43 cases of eosinophilic lymphatic granuloma of head and neck |
JIANG Yang1 HUA Qingquan1 REN Jie1 ZENG Feng1 SHENG Jianfei1 ZHANG Zhijian1 GUAN Hongxia2 YUAN Jingping3 |
1.Department of Otolaryngology Head and Neck Surgery, Renmin Hospital of Wuhan University, Hubei Province, Wuhan 430060, China;
2.Department of Otolaryngology, Hubei Material and Child Health Hospital, Hubei Province, Wuhan 430070, China; 3.Department of Pathology, Renmin Hospital of Wuhan University, Hubei Province, Wuhan 430060, China |
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Abstract Objective To explore the clinical features and diagnosis and treatment of eosinophilic lymphatic granuloma (ELG) of head and neck, in order to improve awareness of the disease in clinicians, reduce the clinical misdiagnosis, missed diagnosis rate and the recurrence rate. Methods The clinical data of 43 patients with ELG of head and neck surgery were confirmed by pathological examination in Renmin Hospital of Wuhan University from July 2000 to January 2017 were collected. The detailed data were summarized, including basic information, clinical symptoms, routine blood tests, imaging examination, pathological examination and recurrence. Results The patients were often treated with recurrent painless swelling as the initial symptom, which could be single or multiple, and could be accompanied by skin itching or pigmentation. The diseased region was mainly in the neck (24 cases), followed by the parotid gland (9 cases). In laboratory examination, eosinophilic granulocytes in 33 cases were significantly elevated, and IgE in 31 cases were increased significantly. 26 cases were treated by simple surgery, with 9 cases recurrence; 13 cases were treated with combined treatment (surgical + radiotherapy or hormone + radiotherapy), with only one case recurrence. Conclusion The main clinical manifestations of ELG are painless mass, increased peripheral blood eosinophils and serum IgE, and its diagnosis relies on pathological examination. Surgical treatment is the preferred treatment, and combined radiotherapy and hormone therapy can reduce recurrence rate.
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[1] Kimm HT,Szeto C. Eosinophilic hyperplastic lymphogranuloma,comparison with Mikulicz's disease [J]. Proc Chin Med Soc,1937,23(3):329.
[2] Kimura T,Yoshimura S,Ishikawa E. On the unusual granulation combined with hyperplastic changes of lymphatic tissue [J]. Trans Soc Pathol Jpn,1948,37(8):179-180.
[3] García CR,Romero BM,Rebollo-Aparicio N,et al. Eosino?鄄philia and multiple lymphadenopathy:Kimura disease,a rare,but benign condition [J]. BMJ Case Rep,2016,31(3):2016.
[4] 张凯,孔玉,刘振丽,等.头颈部多发嗜酸性粒细胞增生性淋巴肉芽肿1例[J].河北医科大学学报,2015,36(10):1124,1133,1138.
[5] 张艳秋,李巍.头颈部嗜酸性粒细胞增生性淋巴肉芽肿5例分析并文献复习[J].基层医学论坛,2016,20(10):1316-1318.
[6] 周俊芬,刘玉林,陈宪,等.木村病的影像表现[J].中华放射学杂志,2014,48(7):601-602.
[7] Zhang R,Ban XH,Mo YX,et al. Kimura′s disease:the CT and MRI characteristics in fifteen cases [J]. Eur J Radiol,2011,80(2):489-497.
[8] Tseng CF,Lin HC,Huang SC,et al. Kimura′s disease presenting as bilateral parotid masses [J]. Eur Arch Otorhinolaryngol,2005,262(12):8-10.
[9] KohH,KamilishN,ChiyotaniA,et al. Eosinophilic lung disease complicated by Kimura′ s disease:a case report and literature review [J]. Intern Med,2012,51(22):3163-3167.
[10] Choi WJ,Hur J,Ko JY,et al. An unusual clinical presentation of Kimura′s disease occurring on the buttock of a five-year-old boy [J]. Ann Dermatol,2010,22(1):57-60.
[11] Fatani HA,Al-Mutrafi A,Al-Qahtani KH,et al. Co-existenceof lip and epiglottis Kimura′s disease [J]. Saudi Med J,2015,36:1226-1228.
[12] Jang S,Lee H,Baek S. Kimura disease presenting as an eyelidmass in a young asian male [J]. J Craniofac Surg,2015, 26(3):e342-e344.
[13] 刘喜玲,袁健,于飞,等.颌面部嗜酸性淋巴肉芽肿的临床病理特点与诊断[J].临床口腔医学杂志,2008,24(8):486-488.
[14] Jin L,Zhang YH,Shi HW. Clinical features and treatment ofeosinophilic lymphoid granuloma in children [J]. J Appl Clin Pediatr,2006,21(21):1489-1490.
[15] Tanaka Y,UenoY,ShimadaY,et al. Paradoxical brain embolismassociated with Kimura disease mimics watershed infarction [J]. J Stroke Cerebrovasc Dis,2015,24(2):55-57.
[16] Lee J,HongYS. Kimura disease complicated with bowel infarctionand multiple arterial thromboses in the extremities [J]. J Clin Rheumatol,2014,20(1):38-41.
[17] Rajpoot DK,Pahl M,Clark J. Nephrotic syndrome associatedwith Kimura disease [J]. Pediatr Nephrol,2000,14(6):486-488.
[18] Helander SD,Peters MS,Kuo TT,et al. Kimuraˊs disease and angiolymphoid hyperplasia with eosinophilia:new observations from immunohistochemical studies of lymphocyte markers,endothelial antigens,and granulocyte proteins [J]. J Cutan Pathol,1995,22(4):319-326.
[19] 杨志寅.现代医学科学发展中的缺憾与思考[J].中华诊断学电子杂志,2013,1(1):1-7.
[20] Hareyama M,Oouchi A,Nagakura H,et al. Radiotherapy for Kimura's disease:the optimum dosage [J]. Int J Radiat Oncol Biol Phys,1998,40(2):647-651.
[21] Liu C,Hu W,Chen H,et al. Clinical and pathologicalstudy of Kimura's disease with renal involvement [J]. JNephrol,2008,21(4):517-525.
[22] Deng WY,Ye SB,Luo RZ,et al. Notch-1 and Ki-67 receptor as predictors for the recurrence and prognosis of Kimura′s disease [J]. Int J Clin Exp Pathol,2014,7(14):2402-2410.
[23] Wai H,Nakae K,Ikeda K,et al. Kimura disease:diagnosis and prognostic factors [J]. Otolaryngol Head Neck Surg,2007,137(23):306-311.
[24] Viswanatha B. Kimura′s disease in children:a 9 years prospective study [J]. Int J Pediatr Otorhinolaryngol,2007, 71(12):1521-1525.
[25] Iwai H,Nakae K,Ikeda K,et al. Kimura disease:diagnosis and prognostic factors [J]. Otolaryngol Head Neck Surg,2007,137(1):306-311.
[26] 陈青立.木村病的复发因素和预后分析及白介素21与22在疾病中的表达与意义[D].乌鲁木齐:新疆医科大学,2016.
[27] 邓维叶,高云飞,陈艳峰,等. Ki-67在木村病患者中的表达和复发相关因素分析[J].中山大学学报:医学科学版,2014,35(4):584-588. |
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